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Lancet (London, England)|March 15, 1986
Deletion on the X chromosome detected by direct DNA analysis in one of two unrelated boys with glycerol kinase deficiency, adrenal hypoplasia, and Duchenne muscular dystrophyD B Dunger, K E Davies, M Pembrey, et al.Archives of Disease in Childhood|June 1, 1980
PseudohypoaldosteronismM J Dillon, J V Leonard, J M Buckler, et al.The Journal of Clinical Endocrinology and Metabolism|September 16, 1999
A novel parathyroid hormone (PTH)/PTH-related peptide receptor mutation in Jansen's metaphyseal chondrodysplasiaE Schipani, C Langman, J Hunzelman, et al.Archives of Disease in Childhood|August 24, 2002
Erythromelalgia: an endothelial disorder responsive to sodium nitroprussideM K H Chan, A T Tucker, S Madden, et al.Kidney International|January 1, 1988
Intravascular platelet activation in the hemolytic uremic syndromeM D Walters, M Levin, C Smith, et al.British Medical Journal|June 22, 1974
Acute respiratory failure in bronchiolitis and pneumonia in infancy. Modes of presentation and treatmentH Simpson, D J Matthew, A H Habel, et al.Archives of Disease in Childhood|October 1, 1983
Survival rates in cystic fibrosisR W Wilmott, S L Tyson, R Dinwiddie, et al.Neuropediatrics|August 1, 1989
EEG monitoring of prolonged thiopentone administration for intractable seizures and status epilepticus in infants and young childrenR C Tasker, S G Boyd, A Harden, et al.Intensive Care Medicine|January 1, 1990
The cerebral function analysing monitor in paediatric medical intensive care: applications and limitationsR C Tasker, S G Boyd, A Harden, et al.Lancet (London, England)|February 12, 1977
Prevention of eczemaD J Matthew, B Taylor, A P Norman, et al.Pageof 22